DHP Topical Anesthetic Gel Recall
DHP Topical Anesthetic Gel (benzocaine 20%, strawberry flavor) is recalled because some bottles may have incomplete seals, which could compromise the product's …
Keystone Industries
Drug & Medication recalls
The newest FDA drug and medication recalls, prescription and over the counter, in plain English. We list the affected lot numbers, the reason for each recall, and whether you should stop taking the product or return it.
133 recalls · updated Jul 16, 2026
IntegraDose Vasopressin Recall
IntegraDose Compounding Services is recalling Vasopressin 2 Units/2 mL syringes because the medication is subpotent, meaning it may not contain the full, …
IntegraDose Compounding Services LLC
Eugia Lidocaine HCl Injection Recall
Eugia is recalling a lidocaine injection because the label wrap covers the barcode, making it difficult to scan. This is a voluntary recall initiated by the …
Eugia US LLC
Spectra Lidocaine HCl Injection Recall
Spectra Medical Devices is recalling Lidocaine HCl Injection because the company cannot guarantee the product is sterile. Non-sterile injectable medications can …
Spectra Medical Devices, Llc
IntegraDose Fentanyl Citrate Injection Recall
IntegraDose Compounding Services is recalling fentanyl citrate sterile injection (2,500 mcg/50mL) because the doses are subpotent, meaning they contain less …
IntegraDose Compounding Services LLC
Safecor Atomoxetine 10mg Recall
Safecor Health is recalling Atomoxetine Capsules labeled as 10 mg because some capsules actually contain 25 mg due to a labeling error. Taking the wrong dose of …
Safecor Health, LLC
Zydus Erythromycin 500 mg Tablets Recall
Zydus Pharmaceuticals is recalling Erythromycin 500 mg tablets because they contain higher-than-safe levels of a potentially harmful chemical. If you take this …
Zydus Pharmaceuticals (USA) Inc
Oasis Tears PF Eye Drops Recall
Oasis Tears PF preservative-free lubricant eye drops are being recalled due to lack of assurance of sterility. Non-sterile eye drops can cause serious eye …
Oasis Medical, Inc.
Lupin Liraglutide Injection Recall
Lupin Pharmaceuticals has recalled Liraglutide Injection 18 mg/3 mL due to the presence of a white thread-like structure found in some cartridges. Using a …
Lupin Pharmaceuticals Inc.
Similasan iVIZIA Eye Drops Recall
Similasan iVIZIA Sterile Lubricant Eye Drops (0.33 fl oz) are being recalled because the manufacturer did not maintain proper sterility safeguards during …
Thea Pharma, Inc.
IVIZIA Lubricant Eye Drops Recall
IVIZIA Sterile Lubricant Eye Drops have been recalled because the FDA found manufacturing safety issues that affect sterility. If you use this product, stop use …
Thea Pharma, Inc.
GenTeal Tears Eye Gel Recall
GenTeal Tears Lubricant Eye Gel is being recalled because the manufacturer cannot assure the product is sterile. Use of a non-sterile eye product can cause …
Alcon Research LLC
FreshKote Lubricant EyeDrops Recall
FreshKote Lubricant EyeDrops are being recalled because the manufacturer cannot guarantee the product's sterility. Non-sterile eyedrops can cause serious eye …
Harrow Eye LLC
Omega-3-Acid Ethyl Esters Capsules Recall
The Harvard Drug Group is recalling Omega-3-Acid Ethyl Esters capsules because the capsule shells failed stability testing and do not meet specifications for …
The Harvard Drug Group LLC
Blaine Labs TERPENICOL Antifungal Solution Recall
Blaine Labs is recalling TERPENICOL Antifungal Solution because the manufacturer stopped required safety testing for products still being sold. The company did …
Blaine Labs Inc
Blaine Labs Fungal Fusion Eradication Kit Recall
Blaine Labs is recalling its Fungal Fusion Eradication Solution antifungal kit because the manufacturer stopped doing required stability testing on products …
Blaine Labs Inc
Apotex Desmopressin Nasal Spray Recall
Apotex is recalling Desmopressin Nasal Spray due to defective bottle caps with dislodged or missing cap liners, which could compromise the integrity of the …
Apotex Corp.
Hikma Alendronate Sodium Recall
Hikma Pharmaceuticals is recalling Alendronate Sodium Oral Solution due to out-of-specification assay results in some bottles that were stored on their side. …
Hikma Pharmaceuticals USA INC
B. Braun Dextrose Injection 70% Recall
B. Braun Medical is recalling Dextrose Injection USP 70% in 2000 mL bags due to a lack of sterility assurance and potential leakage from the diaphragm port. …
B BRAUN MEDICAL INC
Wells Pharma Ketamine Injectable Recall
Ketamine Hydrochloride Injectable Solution 50 mg/mL manufactured by Wells Pharma of Houston has been recalled due to manufacturing quality deviations. Stop …
Wells Pharma of Houston LLC
Wells Pharma Fentanyl Citrate Recall
Wells Pharma is recalling fentanyl citrate injectable solution (2500 mcg/250 mL bags) due to manufacturing process deviations that could affect the product's …
Wells Pharma of Houston LLC
Wells Pharma Fentanyl Citrate Injection Recall
Wells Pharma of Houston is recalling fentanyl citrate injectable solution (NDC 73702-203-65) due to manufacturing quality issues that may affect the drug's …
Wells Pharma of Houston LLC
Epinephrine Injection Recall by Amphastar
International Medication Systems is recalling an epinephrine injection due to lack of assurance of sterility. Sterile injectable medications that are not …
International Medication Systems Ltd.
Appco Pharma Prazosin Recall
Appco Pharma has recalled Prazosin Hydrochloride Capsules 2mg due to detection of a potentially harmful impurity (N-nitroso-prazosin) above acceptable limits. …
Appco Pharma LLC
Prazosin Hydrochloride 1mg Capsules Recall
Prazosin Hydrochloride Capsules, USP 1 mg (100-count bottles) manufactured by Appco Pharma LLC for Biocon Pharma Inc. are being recalled because they contain …
Appco Pharma LLC
Taro Fluocinonide Cream 0.05% Recall
Fluocinonide 0.05% Cream (30g tube) is being recalled because the cream's viscosity (thickness) tested above safe limits during quality testing. This may affect …
SUN PHARMACEUTICAL INDUSTRIES INC
Fagron Vancomycin HCI Injection Recall
Fagron's Vancomycin HCI injection is being recalled because it may not be sterile and a plastic piece on the administration port could break off and enter the …
Fagron Compounding Services
MGC Health Cough Drops Recall
MGC Health Sugar Free Honey Lemon Menthol Cough Drops (25-count bags) are being recalled due to quality concerns identified at the manufacturing facility during …
Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
MGC Health Menthol Cough Drops Recall
MGC Health Menthol Cough Drops in Honey Lemon flavor are being recalled due to quality concerns discovered during a manufacturing facility inspection. The FDA …
Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
Exchange Select Cough Drops Recall
Exchange Select Menthol Cough Drops (30-count bags, Honey Lemon flavor) are being recalled due to manufacturing facility quality concerns discovered during an …
Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
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